HEMOCLAV VENOUS CATHETER— 510(k) K831801

Substantially Equivalent

Exo, Inc.

FDA 510(k) clearance K831801 for HEMOCLAV VENOUS CATHETER, Substantially Equivalent on 1983-07-07. Applicant: Exo, Inc.. Device class: 2.

Clearance details

Applicant: Exo, Inc.
Product code: Code FIQ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1983-06-03
Decision date: 1983-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FIQ

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K892663 — S-100 ALLEN-BROWN SHUNT1989-05-04
K892666 — SAF-T-SHUNT, S-300 SERIES1989-05-04
K844692 — PEDIATRIC SIZED HEMOCATH CATHETER1985-01-18
K841791 — PLUME FISTULA NEEDLE1984-07-09

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Data sourced from openFDA. This site is unofficial and independent of the FDA.